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36397-51-0

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36397-51-0 Usage

General Description

3-(4-METHOXYPHENYL)PROPYLAMINE HCL, also known as 4-Methoxyamphetamine HCl, is a synthetic chemical compound that belongs to the class of organic compounds known as amphetamines and derivatives. These are organic compounds containing or derived from 1-phenylpropan-2-amine. As a salt, it is usually found in a highly stable hydrochloride form (HCL) that enhances its storage and handling. It is often used for research and development purposes, especially in neuropharmacology. The amateur use or misuse of this compound can lead to severe health implications due to its psychoactive properties, and it's therefore legislated under the category of controlled substances in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 36397-51-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,3,9 and 7 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 36397-51:
(7*3)+(6*6)+(5*3)+(4*9)+(3*7)+(2*5)+(1*1)=140
140 % 10 = 0
So 36397-51-0 is a valid CAS Registry Number.

36397-51-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-methoxyphenyl)propan-1-amine,hydrochloride

1.2 Other means of identification

Product number -
Other names 3-(4-methoxyphenyl)propan-1-amine hydrochloride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:36397-51-0 SDS

36397-51-0Relevant articles and documents

Direct Primary Amination of Alkylmetals with NH-Oxaziridine

Behnke, Nicole Erin,Kielawa, Russell,Kwon, Doo-Hyun,Ess, Daniel H.,Kürti, László

supporting information, p. 8064 - 8068 (2019/01/04)

A method for the primary electrophilic amination of primary, secondary, and tertiary organometallic substrates from a bench-stable NH-oxaziridine reagent is described. This facile and highly chemoselective transformation occurs at ambient temperature and without transition metal catalysts or purification by column chromatography to provide alkylamine products in a single step. Density functional theory (DFT) calculations revealed that, despite the basicity of alkylmetals, the direct NH-transfer pathway is favored over proton and O-transfer.

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